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| Sponsor: | National Institute on Aging (NIA) |
|---|---|
| Collaborator: |
Hebrew SeniorLife |
| Information provided by: | National Institute on Aging (NIA) |
| ClinicalTrials.gov Identifier: | NCT00605072 |
Purpose
The purpose of this study is to examine the effects of blood pressure medications on cognition and blood flow in hypertensive elderly patients with cognitive impairment. The hypothesis is that treatment with an angiotensin receptor blocker (ARB) or an angiotensin-converting enzyme inhibitor (ACEI) will be associated with a slower rate of further cognitive decline, improved cerebral blood flow and its regulation, and preserved physical function as compared to treatment with a diuretic (HCTZ), independent of blood pressure level.
| Condition | Intervention | Phase |
|---|---|---|
|
Cognitive Impairment Hypertension Aging |
Drug: candesartan Drug: lisinopril Drug: hydrochlorothiazide Drug: nifedipine, long acting Drug: metoprolol, long-acting |
Phase II |
| Study Type: | Interventional |
| Study Design: | Treatment, Randomized, Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Parallel Assignment, Efficacy Study |
| Official Title: | The Antihypertensives and Vascular, Endothelial and Cognitive Function Trial (AVEC Trial) |
| Estimated Enrollment: | 100 |
| Study Start Date: | January 2008 |
| Estimated Study Completion Date: | December 2011 |
| Estimated Primary Completion Date: | December 2011 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
ARB: Experimental
Angiotensin Receptor Blocker
|
Drug: candesartan
orally 8 mg increased to 16 mg then 32 mg to achieve target blood pressure of 140/90, then daily for 12 months
Drug: nifedipine, long acting
If needed to achieve target blood pressure of 140/90, added to ARB or ACEI at 30 mg increased to 60 mg and 90 mg in 2 week increments
Drug: metoprolol, long-acting
If needed to achieve target blood pressure of 140/90, added to ARB or ACEI at 12.5 mg increased to 25 mg and 50 mg
|
|
ACEI: Experimental
Angiotensin-Converting Enzyme (ACE) Inhibitor
|
Drug: lisinopril
orally 10 mg increased to 20 mg then 40 mg to achieve target blood pressure of 140/90, then daily for 12 months
Drug: nifedipine, long acting
If needed to achieve target blood pressure of 140/90, added to ARB or ACEI at 30 mg increased to 60 mg and 90 mg in 2 week increments
Drug: metoprolol, long-acting
If needed to achieve target blood pressure of 140/90, added to ARB or ACEI at 12.5 mg increased to 25 mg and 50 mg
|
| HCTZ: Active Comparator |
Drug: hydrochlorothiazide
orally 12.5 mg increased to 25 mg to achieve target blood pressure of 140/90, then daily for 12 months
|
There is mounting evidence that hypertension, which affects more than 65% of the US elderly population, accelerates cognitive decline and increases the risk of functional disability among older individuals. Hypertension is also associated with cerebral blood flow reduction and dysregulation which contribute to further cognitive and functional impairment. Drugs that inhibit angiotensin II (ACEI and ARB) are commonly used antihypertensives and may have a protective effect on cognitive function, cerebral blood flow and physical function compared to other antihypertensives such as hydrochlorothiazide (HCTZ).
A total of 100 individuals will be recruited for this pilot 3-arm randomized study to investigate the effects of: (i) 12 months treatment with candesartan (ARB) compared to hydrochlorothiazide (HCTZ) and (ii) 12 months treatment with lisinopril (ACEI) compared to HCTZ and (iii) to estimate the effect size difference between lisinopril and losartan on cognition, cerebral blood flow regulation, and functional measures in a sample of elderly hypertensive individuals with objective evidence of cognitive impairment.
Eligibility| Ages Eligible for Study: | 60 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Contacts and Locations| Contact: Meaghan Hart | 617-363-8484 | MeaghanHart@hrca.harvard.edu |
| United States, Massachusetts | |
| Institute for Aging Research at Hebrew SeniorLife | Recruiting |
| Boston, Massachusetts, United States, 02131 | |
| Contact: Meaghan Hart 617-363-8484 MeaghanHart@hrca.harvard.edu | |
| Principal Investigator: Ihab Hajjar, MD, MS | |
| Sub-Investigator: Lewis Lipsitz, MD | |
| Principal Investigator: | Ihab Hajjar, MD | Hebrew SeniorLife |
More Information
| Responsible Party: | Hebrew SeniorLife ( Ihab Hajjar, MD ) |
| Study ID Numbers: | IA0127, 1K23AG30057-01A1 |
| Study First Received: | January 11, 2008 |
| Last Updated: | September 9, 2009 |
| ClinicalTrials.gov Identifier: | NCT00605072 History of Changes |
| Health Authority: | United States: Federal Government |
|
cognitive disorders |
|
Vasodilator Agents Neurotransmitter Agents Adrenergic Agents Molecular Mechanisms of Pharmacological Action Cardiotonic Agents Sodium Chloride Symporter Inhibitors Diuretics Physiological Effects of Drugs Calcium Channel Blockers Reproductive Control Agents Nifedipine Membrane Transport Modulators Tocolytic Agents Mental Disorders Therapeutic Uses |
Angiotensin-Converting Enzyme Inhibitors Adrenergic beta-Antagonists Cardiovascular Diseases Anti-Arrhythmia Agents Sympatholytics Lisinopril Vascular Diseases Enzyme Inhibitors Cardiovascular Agents Metoprolol Antihypertensive Agents Protective Agents Hydrochlorothiazide Cognition Disorders Pharmacologic Actions |